S5702 Post-Hepatectomy Portal Hypertensive Sequelae Treated With Splenic Embolization and Complicated by Formation of a Large Splenic Pseudocyst

Introduction: A Klatskin tumor is a rare malignancy occurring at the common hepatic duct bifurcation. About two-thirds of Klatskin tumors are resectable, often requiring bile duct resection and less commonly partial hepatectomy. Post-hepatectomy portal hypertension (PHPH) is a known complication with high morbidity and mortality. We present a case of a patient with PHPH who underwent splenic embolization, leading to the rare formation of a large symptomatic splenic pseudocyst. Case Description/Methods: Fifty-seven-year-old man with history of a Klatskin tumor status post partial right hepatectomy presented with syncope, coffee ground emesis, and melena. Labs were significant for Hb 6.0, Hct 21.3, MCV 74.2, PLT 212, aspartate aminotransferase 39, alanine aminotransferase 37, alkaline phosphatase 226, total bilirubin 1.0, international normalized ratio 1.2. Computed tomography (CT) imaging revealed chronic extrahepatic main portal vein occlusion with cavernous transformation, absent middle hepatic vein, gastrorenal shunt, gastric and esophageal varices, and splenomegaly. Esophagogastroduodenoscopy confirmed gastric and esophageal varices with a large IGV1 gastric varix with high risk bleeding stigmata. Due to the complex anatomy, a transjugular intrahepatic portosystemic shunt (TIPS) procedure was deemed high risk. Coil-assisted or balloon-occluded retrograde transvenous obliteration (CRTO/BRTO) of the gastrorenal shunt was considered, but carried risk of worsening the patient’s esophageal varices. Ultimately, the patient underwent splenic artery embolization (50%-60%) to reduce portal pressures and decrease re-bleeding risk. Two months later, the patient presented with left sided abdominal pain, vomiting, and a left pleural effusion. MRI showed an 18 × 21 × 23 cm splenic pseudocyst. A percutaneous drain was placed. Fluid cultures grew Enterococcus faecalis, treated with daptomycin. Discussion: PHPH is linked to poorer long-term survival and an increased post-hepatectomy liver failure. The development of PHPH can be predicted by the extent of the liver resection, with larger hepatectomies carrying higher risk. As seen in this case, understanding postsurgical anatomy and portosystemic changes is crucial when planning intervention. Splenic artery embolization is a minimally invasive approach to variceal bleeding, but it is not without risk. Post-embolization symptoms of nausea, vomiting, abdominal pain should be addressed promptly to reduce complications associated with pseudocysts - including superinfections of the cystic fluid. The challenges associated with PHPH and its management present a promising area for further research.

Publication Details

Journal
The American Journal of Gastroenterology
Published
2025-10-01
DOI
https://doi.org/10.14309/01.ajg.0001150268.36772.55
Primary Topic
Liver Disease and Transplantation
Type
article
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article

S5702 Post-Hepatectomy Portal Hypertensive Sequelae Treated With Splenic Embolization and Complicated by Formation of a Large Splenic Pseudocyst

The American Journal of Gastroenterology
Liver Disease and Transplantation
article

S5702 Post-Hepatectomy Portal Hypertensive Sequelae Treated With Splenic Embolization and Complicated by Formation of a Large Splenic Pseudocyst

article en

Abstract

Introduction: A Klatskin tumor is a rare malignancy occurring at the common hepatic duct bifurcation. About two-thirds of Klatskin tumors are resectable, often requiring bile duct resection and less commonly partial hepatectomy. Post-hepatectomy portal hypertension (PHPH) is a known complication with high morbidity and mortality. We present a case of a patient with PHPH who underwent splenic embolization, leading to the rare formation of a large symptomatic splenic pseudocyst. Case Description/Methods: Fifty-seven-year-old man with history of a Klatskin tumor status post partial right hepatectomy presented with syncope, coffee ground emesis, and melena. Labs were significant for Hb 6.0, Hct 21.3, MCV 74.2, PLT 212, aspartate aminotransferase 39, alanine aminotransferase 37, alkaline phosphatase 226, total bilirubin 1.0, international normalized ratio 1.2. Computed tomography (CT) imaging revealed chronic extrahepatic main portal vein occlusion with cavernous transformation, absent middle hepatic vein, gastrorenal shunt, gastric and esophageal varices, and splenomegaly. Esophagogastroduodenoscopy confirmed gastric and esophageal varices with a large IGV1 gastric varix with high risk bleeding stigmata. Due to the complex anatomy, a transjugular intrahepatic portosystemic shunt (TIPS) procedure was deemed high risk. Coil-assisted or balloon-occluded retrograde transvenous obliteration (CRTO/BRTO) of the gastrorenal shunt was considered, but carried risk of worsening the patient’s esophageal varices. Ultimately, the patient underwent splenic artery embolization (50%-60%) to reduce portal pressures and decrease re-bleeding risk. Two months later, the patient presented with left sided abdominal pain, vomiting, and a left pleural effusion. MRI showed an 18 × 21 × 23 cm splenic pseudocyst. A percutaneous drain was placed. Fluid cultures grew Enterococcus faecalis, treated with daptomycin. Discussion: PHPH is linked to poorer long-term survival and an increased post-hepatectomy liver failure. The development of PHPH can be predicted by the extent of the liver resection, with larger hepatectomies carrying higher risk. As seen in this case, understanding postsurgical anatomy and portosystemic changes is crucial when planning intervention. Splenic artery embolization is a minimally invasive approach to variceal bleeding, but it is not without risk. Post-embolization symptoms of nausea, vomiting, abdominal pain should be addressed promptly to reduce complications associated with pseudocysts - including superinfections of the cystic fluid. The challenges associated with PHPH and its management present a promising area for further research.

The American Journal of GastroenterologyVol. 120(10S2)
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Liver Disease and Transplantation
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